Evidence map›Paper›PMID 35744849›Full record

ArticleMolecules (Basel, Switzerland)2022

Synthesis and Biological Evaluation of Novel Synthetic Indolone Derivatives as Anti-Tumor Agents Targeting p53-MDM2 and p53-MDMX.

Yali Wang, Bo Ji, Zhongshui Cheng, Lianghui Zhang, Yingying Cheng, Yingying Li, Jin Ren, Wenbo Liu, Yuanyuan Ma

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Yali WangSchool of Pharmacy and Life Sciences, Jiujiang University, Jiujiang 332000, China.
Bo JiSchool of Pharmacy and Life Sciences, Jiujiang University, Jiujiang 332000, China.
Zhongshui ChengSchool of Pharmacy and Life Sciences, Jiujiang University, Jiujiang 332000, China.
Lianghui ZhangSchool of Pharmacy and Life Sciences, Jiujiang University, Jiujiang 332000, China.
Yingying ChengSchool of Pharmacy and Life Sciences, Jiujiang University, Jiujiang 332000, China.
Yingying LiSchool of Pharmacy and Life Sciences, Jiujiang University, Jiujiang 332000, China.
Jin RenSchool of Pharmacy and Life Sciences, Jiujiang University, Jiujiang 332000, China.
Wenbo LiuSchool of Pharmacy and Life Sciences, Jiujiang University, Jiujiang 332000, China.
Yuanyuan MaInstitute of Medicinal Biotechnology, Chinese Academy of Medical Science and Peking Union Medical College, Beijing 100050, China.
Jiujiang University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

Jiangxi Provincial Natural Science Foundation 20202BABL216077, 20192BAB215043National Natural Science Foundation of China 21867013, 81860631, 21967013
6 · The paper itself

Abstract

A series of novel indolone derivatives were synthesized and evaluated for their binding affinities toward MDM2 and MDMX. Some compounds showed potent MDM2 and moderate MDMX activities. Among them, compound A13 exhibited the most potent affinity toward MDM2 and MDMX, with a

Indexed as

Antineoplastic AgentsProto-Oncogene Proteins c-mdm2Cell Cycle ProteinsProtein BindingTumor Suppressor Protein p53Antineoplastic AgentsCell Cycle ProteinsProto-Oncogene Proteins c-mdm2Tumor Suppressor Protein p53anti-tumorindolone derivativesp53-MDM2p53-MDMX

Identifiers

PMID35744849
PMCPMC9230548
OpenAlexW4282841661

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.